Amanote Research
Register
Sign In
Discover open access scientific publications
Search, annotate, share and cite publications
Publications by Orsolya-Adrienn Rácz
GP56 Severe Hypercalcemic Crisis in an Infant With Idiopathic Infantile Hypercalcemia Caused by Mutation in CYP24A1 Gene
P122 Celiac Disease Associated With Depression in Adolescents
Related publications
Benign Infantile Epilepsy Mimicking Reflex Anoxic Seizures in an Infant With PRRT2 Gene Mutation
Indian Journal of Pediatrics
Child Health
Pediatrics
Perinatology
Rare LPL Gene Missense Mutation in an Infant With Hypertriglyceridemia
Journal of Clinical Laboratory Analysis
Allergy
Immunology
Biochemistry
Public Health
Medical Laboratory Technology
Clinical Biochemistry
Hematology
Microbiology
Environmental
Occupational Health
A Novel Germline Inactivating Mutation in the CASR Gene in an Italian Kindred Affected by Familial Hypocalciuric Hypercalcemia
European Journal of Endocrinology
Medicine
Endocrinology
Metabolism
Diabetes
Hypercalcemic Crisis. Clinical Case
Opuholi Golovy i Sei
Oncology
Radiology
Pharmacology
Cancer Research
Nuclear Medicine
Otorhinolaryngology
Imaging
Surgery
Multisystem Fatal Infantile Disease Caused by a Novel Homozygous EARS2 Mutation
Brain
Medicine
Neurology
Primary Hyperparathyroidism Presumably Caused by Chronic Parathyroiditis Manifesting From Hypocalcemia to Severe Hypercalcemia
Internal Medicine
Internal Medicine
Medicine
Uncommon Cribfellows: An Infant With Hypercalcemia, Nephrocalcinosis, and Acidosis: Questions
Pediatric Nephrology
Child Health
Pediatrics
Perinatology
Nephrology
Septal Myectomy for Severe Neonatal Hypertrophic Cardiomyopathy Caused by PTPN11 Gene Mutation: A Case Report
Biomedical Journal of Scientific & Technical Research
A Rare Case Report of Immobility-Induced Hypercalcemia in an Infant
Pediatrics
Child Health
Pediatrics
Perinatology
